Motor neurons physical muscular atrophy spinal. Medical search. Frequent questions

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Anatomy72

Motor Neurons Spinal Cord Neurons Anterior Horn Cells Neurons, Afferent Motor Cortex Axons Spinal Nerve Roots Muscle, Skeletal Spinal Nerves Neuromuscular Junction Coiled Bodies Chromosomes, Human, Pair 5 Ganglia, Spinal Synapses Brain Cells, Cultured Interneurons Ganglia, Invertebrate Muscles Spinal Canal Central Nervous System Cholinergic Neurons Sensory Receptor Cells Peripheral Nerves Dendrites Brain Stem Cerebral Cortex Dopaminergic Neurons Sciatic Nerve Hippocampus Inclusion Bodies GABAergic Neurons Neurites Afferent Pathways Facial Nerve Growth Cones Medulla Oblongata Ulnar Nerve Nerve Net Lumbosacral Region Neuroglia Posterior Horn Cells Cerebellum Neurons, Efferent Astrocytes Chick Embryo Ganglia Arm Sural Nerve Cell Line Muscle Fibers, Skeletal Spine Rhombencephalon Spliceosomes Intranuclear Inclusion Bodies Olfactory Receptor Neurons Neural Pathways Efferent Pathways Hindlimb Nociceptors Mesencephalon Nervous System Cervical Vertebrae Pyramidal Cells Pyramidal Tracts Thoracic Vertebrae HeLa Cells Extremities Fibroblasts Presynaptic Terminals Cranial Nerves

Organisms14

Mice, Transgenic Animals, Newborn Rats, Sprague-Dawley Mice, Inbred C57BL Mice, Knockout Animals, Genetically Modified Aplysia Cats Rats, Wistar Mice, Neurologic Mutants Zebrafish Grasshoppers Mice, Mutant Strains Leeches

Diseases44

Muscular Atrophy, Spinal Spinal Muscular Atrophies of Childhood Atrophy Muscular Atrophy Motor Neuron Disease Muscular Disorders, Atrophic Bulbo-Spinal Atrophy, X-Linked Spinal Cord Injuries Amyotrophic Lateral Sclerosis Spinal Cord Diseases Disease Models, Animal Nerve Degeneration Neuromuscular Diseases Optic Atrophy Bulbar Palsy, Progressive Multiple System Atrophy Spinal Cord Neoplasms Spinal Cord Compression Spinal Diseases Muscle Weakness Charcot-Marie-Tooth Disease Spinal Neoplasms Arthrogryposis Spinal Stenosis Fasciculation Paralysis Contracture Spinal Cord Ischemia Olivopontocerebellar Atrophies Neuromuscular Junction Diseases Hereditary Sensory and Motor Neuropathy Vocal Cord Paralysis Spinal Injuries Paraplegia Gyrate Atrophy Pain Neurodegenerative Diseases Disease Progression Geographic Atrophy Movement Disorders Postpoliomyelitis Syndrome Nervous System Diseases Myoclonic Epilepsies, Progressive Respiratory Paralysis

Chemicals and Drugs31

Survival of Motor Neuron 1 Protein SMN Complex Proteins Survival of Motor Neuron 2 Protein Neuronal Apoptosis-Inhibitory Protein Cyclic AMP Response Element-Binding Protein Nerve Tissue Proteins RNA-Binding Proteins Ribonucleoproteins, Small Nuclear DEAD Box Protein 20 snRNP Core Proteins Receptors, Androgen Molecular Motor Proteins Superoxide Dismutase Neurofilament Proteins Green Fluorescent Proteins RNA, Messenger gamma-Aminobutyric Acid Glycine-tRNA Ligase Choline O-Acetyltransferase Neuropeptides Glutamic Acid Neuroprotective Agents Nerve Growth Factors Dopamine Serotonin Transcription Factors Homeodomain Proteins FMRFamide Peptides Calcium DNA Primers

Analytical, Diagnostic and Therapeutic Techniques and Equipment33

Disease Models, Animal Electromyography Injections, Spinal Electric Stimulation Immunohistochemistry Anesthesia, Spinal Pedigree Analysis of Variance Patch-Clamp Techniques Magnetic Resonance Imaging Heterozygote Detection Models, Neurological Physical Therapy Modalities Spinal Fusion Rotarod Performance Test Physical Stimulation Cell Count Models, Biological Muscle Denervation Reflex Blotting, Western Muscle Strength Myelography In Situ Hybridization Axotomy Hand Strength Laminectomy Chromosome Mapping Severity of Illness Index Reverse Transcriptase Polymerase Chain Reaction Polymerase Chain Reaction Brain Mapping Genetic Therapy

Psychiatry and Psychology8

Motor Activity Behavior, Animal Motor Skills Disorders Reaction Time Reflex Psychomotor Performance Functional Laterality Pain

Phenomena and Processes58

Motor Activity Evoked Potentials, Motor Action Potentials Exons Chromosomes, Human, Pair 5 Neural Conduction Mutation Time Factors Phenotype Synaptic Transmission Movement Physical Fitness Locomotion Neural Inhibition Gene Deletion Homozygote Membrane Potentials Gene Expression Regulation Nerve Regeneration RNA Splicing Neuronal Plasticity Evoked Potentials Axonal Transport Cell Differentiation Cell Count Reaction Time Base Sequence Trinucleotide Repeat Expansion Signal Transduction Exercise Cell Survival Excitatory Postsynaptic Potentials Gene Expression Regulation, Developmental Reflex Psychomotor Performance Amino Acid Sequence Recovery of Function Genes, Dominant Genetic Linkage Genes, Recessive Gene Dosage Functional Laterality Gene Expression Dose-Response Relationship, Drug Periodicity Mutation, Missense Pain Muscle Strength Alternative Splicing Neurogenesis Trinucleotide Repeats Cell Death Hand Strength Protein Binding Aging Recruitment, Neurophysiological Muscle Contraction Physical Exertion

Disciplines and Occupations2

Immunohistochemistry Electrophysiology

Anthropology, Education, Sociology and Social Phenomena2

Physical Fitness Exercise

Information Science3

Molecular Sequence Data Base Sequence Amino Acid Sequence

Health Care5

Physical Fitness Analysis of Variance Age Factors Age of Onset Severity of Illness Index

Anatomy Organisms Diseases Chemicals and Drugs Analytical, Diagnostic and Therapeutic Techniques and Equipment Psychiatry and Psychology Phenomena and Processes Disciplines and Occupations Anthropology, Education, Sociology and Social Phenomena Information Science Health Care

Muscular Atrophy, Spinal Spinal Muscular Atrophies of Childhood Motor Neurons Survival of Motor Neuron 1 Protein SMN Complex Proteins Survival of Motor Neuron 2 Protein Atrophy Spinal Cord Muscular Atrophy Motor Neuron Disease Neurons Muscular Disorders, Atrophic Bulbo-Spinal Atrophy, X-Linked Spinal Cord Injuries Anterior Horn Cells Neuronal Apoptosis-Inhibitory Protein Cyclic AMP Response Element-Binding Protein Nerve Tissue Proteins Neurons, Afferent Motor Activity Amyotrophic Lateral Sclerosis RNA-Binding Proteins Motor Cortex Evoked Potentials, Motor Axons Spinal Cord Diseases Disease Models, Animal Ribonucleoproteins, Small Nuclear Nerve Degeneration Neuromuscular Diseases DEAD Box Protein 20 Mice, Transgenic Spinal Nerve Roots Electromyography Action Potentials Optic Atrophy Bulbar Palsy, Progressive Muscle, Skeletal Spinal Nerves Exons Neuromuscular Junction Coiled Bodies Injections, Spinal Chromosomes, Human, Pair 5 Ganglia, Spinal Neural Conduction Mutation Electric Stimulation Synapses Time Factors Brain Cells, Cultured snRNP Core Proteins Immunohistochemistry Phenotype Multiple System Atrophy Interneurons Receptors, Androgen Molecular Motor Proteins Anesthesia, Spinal Electrophysiology Animals, Newborn Synaptic Transmission Movement Physical Fitness Superoxide Dismutase Ganglia, Invertebrate Pedigree Spinal Cord Neoplasms Muscles Spinal Canal Spinal Cord Compression Spinal Diseases Neurofilament Proteins Muscle Weakness Rats, Sprague-Dawley Central Nervous System Mice, Inbred C57BL Cholinergic Neurons Locomotion Charcot-Marie-Tooth Disease Mice, Knockout Animals, Genetically Modified Sensory Receptor Cells Spinal Neoplasms Molecular Sequence Data Peripheral Nerves Neural Inhibition Dendrites Brain Stem Cerebral Cortex Aplysia Analysis of Variance Patch-Clamp Techniques Magnetic Resonance Imaging Dopaminergic Neurons Arthrogryposis Gene Deletion Heterozygote Detection Sciatic Nerve

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